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Trial registered on ANZCTR
Registration number
ACTRN12610000324011
Ethics application status
Approved
Date submitted
6/04/2010
Date registered
21/04/2010
Date last updated
21/04/2010
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effectiveness of the multi-component tailored intervention in treatment of behavioral and psychological symptoms in dementia (BPSD).
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Scientific title
The multi-component tailored intervention in treatment of demented residents with behavioral and psychological symptoms in dementia (BPSD) to alleviate symptoms. Randomized controlled trial.
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Secondary ID [1]
251625
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Behavioral and psychological symptoms in dementia (BPSD)
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Condition category
Condition code
Neurological
257252
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0
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Dementias
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention duration: 14 months. The staff in the intervention wards is supported by the mentor nurse and consulting geriatrician to find the underlying multiple interacting causes of each resident’s behaviour, and to provide individually tailored, comprehensive and multi-component intervention. The intervention is tailored on basis on care wards. Mentor nurse and geriatrician are available on daily basis but actual freqencies and times are based on needs of wards. Mentoring takes place on a one to one basis and in group meetings. Tailoring is the very important principle of intervention
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Intervention code [1]
256264
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Other interventions
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Comparator / control treatment
Two training sessions ( two afternoons, 4 hr each) with a neurology and a gerontologist nurse (not with the mentor) about BPSD are arranged to the staff in control wards. There were lectures regarding to diseases causing dementia and medical and nursing care of dementia
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Control group
Active
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Outcomes
Primary outcome [1]
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1. Alleviation of BPSD among the residents with BPSD. The study nurse collects data with different methods at baseline, 6 months and 14 months by interviewing each resident's primary nurse. Method for BPSD is Neuropsychiatric Interventory- nursing home version (NPI-NH)
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Assessment method [1]
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Timepoint [1]
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14 months (the end of the study period)
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Secondary outcome [1]
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Prevalence and severity of BPSD in the study wards. Data of BPSD with NPI-NH are collected by the study at baseline and 14 months from all the residents in each ward.
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Assessment method [1]
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Timepoint [1]
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14 months (the end of the study period)
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Secondary outcome [2]
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Use of medication
The study nurse collects the lists of medication of each reidents at baseline, 6 and 14 months.
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Assessment method [2]
263794
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Timepoint [2]
263794
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14 months (the end of the study period)
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Secondary outcome [3]
263795
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Well-being of residents with dementia is assessed by two proxy methods. Quality of Life in Late Stage Dementia (QUALID) is collected by the study nurse at baseline, 6 and 14 months. Furthermore, Quality of Life in Dementia Observation tool (ELO-D) is used by two trained ELO-D users during eight hours (10 am-6 pm) in one day, at baseline and 14 months.
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Assessment method [3]
263795
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Timepoint [3]
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14 months (the end of the study period)
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Eligibility
Key inclusion criteria
Resident with dementia (with specific etiological diagnosis) and with BPSD
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Minimum age
50
Years
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Maximum age
100
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Resident is entered to terminal care or is planned to be transferred to another care unit or home
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
All long term care wards in the City of Espoo are participated in the study. Allocation was done by central randomization by computer
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Random order generation: blocked randomization
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/01/2009
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
400
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Finland
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State/province [1]
2570
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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The Slot Machine Association of finland
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Address [1]
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Turuntie 42, 02650 Espoo, Finland
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Country [1]
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Finland
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Primary sponsor type
Charities/Societies/Foundations
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Name
The Central Union for the Welfare of the Aged
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Address
Malmin kauppatie 26, 00700 Helsinki, Finland
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Country
Finland
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Secondary sponsor category [1]
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Government body
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Name [1]
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The National Institute for Health and Welfare (THL)
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Address [1]
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P.O. Box 30, FI-00271 Helsinki, Finland
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Country [1]
256045
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Finland
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Secondary sponsor category [2]
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University
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Name [2]
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University of Eastern Finland
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Address [2]
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P.O. Box 1627
FI-70211 Kuopio, Finland
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Country [2]
256046
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Finland
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Other collaborator category [1]
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University
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Name [1]
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Sibelius Academy
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Address [1]
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P.O.Box 86
FIN-00251 Helsinki, Finland
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Country [1]
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Finland
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Other collaborator category [2]
1189
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Charities/Societies/Foundations
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Name [2]
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The Age Institute
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Address [2]
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Kalevankatu 12 A, 00100 Helsinki, Finland
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Country [2]
1189
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Finland
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Other collaborator category [3]
1190
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Charities/Societies/Foundations
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Name [3]
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The Society of Memory Disorders expertise in Finland
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Address [3]
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Fredriksberginkatu 2
00240 Helsinki, Finland
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Country [3]
1190
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Finland
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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The Ethic Committee of Hospital District of Helsinki and Uusimaa
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Ethics committee address [1]
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Biomedicum Helsinki 2 C, PL 705, 00029 HUS, Finland
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Ethics committee country [1]
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Finland
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Date submitted for ethics approval [1]
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12/04/2008
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Approval date [1]
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06/06/2008
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Ethics approval number [1]
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153/13/03/00/08
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Summary
Brief summary
The primary purpose of the study is to determine if a multicomponent support program coordinated by a mentor nurse is efficient in alleviating BPSD. The hypothesis is (1) that there are various kinds of triggering factors for BPSD and treatment solututions may be found by supporting personnel systematically and multiprofessionally to understand those triggering factors and (2) that care provided in these grounds alleviates BPSD
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Trial website
www.mielenmuutos.fi -> Dementia Study
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
31021
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Country
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Phone
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Fax
31021
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Email
31021
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Contact person for public queries
Name
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Ulla Eloniemi-Sulkava
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Address
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The Central Union for the Welfare of the Aged
Malmin kauppatie 26
00700 Helsinki, Finland
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Country
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Finland
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Phone
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+358 50 5180907
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Fax
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+350 9 350 86010
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Email
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[email protected]
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Contact person for scientific queries
Name
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Ulla Eloniemi-Sulkava
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Address
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The Central Union for the Welfare of the Aged
Malmin kauppatie 26
00700 Helsinki, Finland
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Country
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Finland
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Phone
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+358 50 5180907
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Fax
5196
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+350 9 350 86010
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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